نتایج جستجو برای: major ß thalassemia

تعداد نتایج: 639703  

Journal: :iranian red crescent medical journal 0
mohammad ali mashhadi department of hematology and oncology, ali ebne abitaleb hospital, zahedan university of medical sciences, zahedan, ir iran zahra sepehri department of internal medicine, amir al-momenin hospital, zabol university of medical sciences, zabol, ir iran; department of internal medicine, amir al-momenin hospital, zabol university of medical sciences, zabol, ir iran. tel: +98-9126880468 zahra heidari department of internal medicine, ali ebne abitaleb hospital, zahedan university of medical sciences, zahedan, ir iran eghbal shirzaee department of internal medicine, ali ebne abitaleb hospital, zahedan university of medical sciences, zahedan, ir iran zohre kiani kerman university of medical sciences, kerman, ir iran

background there are different and controversial reports about zinc deficiency in patients with major thalassemia. objectives the aim of this study was to evaluate zinc status in patients with major thalassemia in sistan and baluchistan province, southeastern iran. patients and methods the study was performed in ali asghar hospital, a specialized governmental hospital located in zahedan, iran. ...

Journal: :The Professional Medical Journal 2018

Journal: :iranian journal of allergy, asthma and immunology 0
ahmad tamaddoni iraj mohammadzadeh omid ziaei

β- thalassemia major is a common hemoglobinopathy in humans. in some journals, numerous studies have reported different prevalence of hepatitis c among β- thalassemia major because thalassemic patients need multiple blood transfusions and blood transfusion is a common transmission pathway for hepatitis c virus. thus this study was performed for detection of anti-hcv between β- thalassemia major...

Journal: :journal of research in medical sciences 0
giuseppina messina hereditary anemia center, dept internal medicine, policlinico foundation irccs, university of milan, italy elisa colombo unit of psychiatry, policlinico foundation irccs, university of milan, italy elena cassinerio hereditary anemia center, dept internal medicine, policlinico foundation irccs, university of milan, italy claudia cesaretti hereditary anemia center, dept internal medicine, policlinico foundation irccs, university of milan, italy alessia marcon hereditary anemia center, dept internal medicine, policlinico foundation irccs, university of milan, italy laura zanaboni hereditary anemia center, dept internal medicine, policlinico foundation irccs, university of milan, italy

background: the reproductive and sexual health issues concerning persons affected by thalassemia major are complex. the study was planned to investigate the psychological attitudes and expectations in a group of thalassemic pregnant women attending hospital for regular blood transfusion. methods : this is a preliminary cross-sectional study involving 20 consecutive thalassemic patients and a co...

Journal: :iranian journal of pediatric hematology and oncology 0
bijan keikhaei department of pediatrics, research center for thalassemia & hemoglobinopathy, joundishapur university of medical science

abstract background iron overload is a major problem in patients with major thalassemia. an effective and safe iron chelator protocol with high compliance rate plays an important role in treatment of these patients. this study was done to assess the efficacy and safety of the sequential deferoxamine and deferasirox protocol in major thalassemia patients in khuzestan province, iran. material and...

2009
P. Pimol Chiewsilp S. Suthat Fucharoen

Suntaree Apibal, Department of Pathology, Faculty of Medicine, Ramathibodi Hospital, Bangkok 10400 (Thailand) The presence of fetal red cells (F cells) in the maternal circulation is an indicator of a fetomaternal hemorrhage which may subsequently lead to hemo-lytic disease of the newborn [1]. However, a small amount of F cells were found in some normal adults [4] whereas the increase in hemogl...

2003
Ghazi O. Tadmouri

aid in the analysis of data, and (c) the interpretation of results in a biomedically meaningful manner.1 To fulfill these aims, vast amounts of information are stored in information repositories called databases. Database types differ considerably depending, primarily, on the nature of the information stored. In biomedical applications, the hierarchical and relational schemes are widely used. A...

Journal: :international journal of hematology-oncology and stem cell research 0
amir ali hamidieh pediatric hematology- oncology and stem cell transplantation department, hematology- oncology and stem cell transplantation research center, shariati hospital, tehran university of medical sciences, tehran, iran b moradbeag faculty of medicine, qom islamic azad university, qom, iran f pasha faculty of medicine, tehran islamic azad university, tehran, iran mehdi jalili pediatric hematology- oncology and stem cell transplantation department, ematology- oncology and stem cell transplantation research center, shariati hospital, tehran university of medical sciences, tehran, iran m hadjibabaie clinical pharmacology department, faculty of pharmacy, tehran university of medical sciences, tehran, iran m keshavarznia faculty of medicine, qom islamic azad university, qom, iran

introduction: hypoparathyroidism (hpt) is an irreversible but preventable disorder caused by an iron overload which can be considered a typical complication in patients with beta-thalassemia major. patients and method: parathyroid function was evaluated in 130 patients in qom, iran, who suffered from beta-thalassemia major. their serum ferritin levels were checked for monitoring of chelation th...

Journal: :international journal of hematology-oncology and stem cell research 0
fereshteh maryami biotechnology research center, department of molecular medicine, pasteur institute of iran, tehran, iran azita azarkeivan pediatric hematology oncology, transfusion research center, high institute for research and education in transfusion medicine, department of thalassemia clinic, tehran, iran mohammad sadegh fallah kawsar human genetics research center, tehran, iran sirous zeinali iranian molecular medicine network, biotechnology research center, pasteur institute of iran, pasteur st, tehran, iran kawsar human genetics research center, tehran, iran

background: thalassemia syndromes are the most prevalent single gene disorders in iran. this study aimed to evaluate the effect of different types of beta-globin gene mutations, co-inheritance of alpha-globin gene mutations and/or xmn1 snp on disease phenotype in a large cohort of iranian patients. subjects and methods: in total, 433 patients were clinically classified into β-thalassemia major ...

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